H. Nmr, ? (ppm): 8.54 (d, J = 4.8 Hz, 1H)99 (s, 1H), 1H), 7.29 (m, 5H), 6.48 (d, J = 4.8 Hz, 1H), 4.54 (s, 2H), 3.59 (s, 2H), p.54

. Hz, 13 C NMR (CDCl 3 ), ? (ppm): 152(diethylamino)methyl)benzyl)quinolin-4-amine (3) was prepared by an analogous procedure using, pp.7-11, 17610.

. Anal, ESI-MS (M+H + ) = 354-((diethylamino)methyl)-[1,1'-biphenyl]-4-yl)methyl)quinolin-4-amine (4) was prepared by an analogous procedure using N-((4'-(aminomethyl)-[1,1'-biphenyl]-4-yl) methyl)-N,N-diethylamine (9) (7.8 g, 276 g, 174 mmol), triethylamine (26 mL, 189 mmol), and NMP (30 mL) The resulting product (light yellow powder) was dried under vacuum95 (s, 1H), ), 2.54 (q, J = 7.2 Hz, 4H), 1.09 (t, J = 7.2 Hz, 6H). 13 C NMR (CDCl 3 )81. ESI-MS (M+H + ) = 430, pp.16588-354, 19718.

6. Hz, 13 C NMR, p.1877

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